Heparanase
Heparanase
Heparanase is an endo-β-D-glucuronidase enzyme that specifically cleaves heparan sulfate (HS) side chains of heparan sulfate proteoglycans (HSPGs) in the extracellular matrix (ECM) and on cell surfaces. This enzymatic activity is crucial in the remodeling of the ECM and is implicated in various physiological and pathological processes, including tumor metastasis, angiogenesis, and inflammation.
Structure
Heparanase is synthesized as a latent 65 kDa precursor that undergoes proteolytic processing to yield an active heterodimer composed of an 8 kDa and a 50 kDa subunit. The active site of heparanase is located within the 50 kDa subunit, which contains the catalytic residues necessary for its enzymatic function.
Function
Heparanase degrades heparan sulfate chains by cleaving the β(1→4) glycosidic bond between glucuronic acid and glucosamine residues. This activity results in the release of bioactive molecules sequestered within the ECM, such as growth factors and cytokines, thereby modulating cell behavior and tissue dynamics.
Role in Cancer
Heparanase is overexpressed in many types of cancer, where it facilitates tumor cell invasion and metastasis by degrading the ECM and basement membranes. This degradation allows cancer cells to penetrate tissue barriers and spread to distant sites. Additionally, heparanase activity promotes angiogenesis by releasing angiogenic factors like vascular endothelial growth factor (VEGF).
Role in Inflammation
In the context of inflammation, heparanase contributes to leukocyte extravasation by remodeling the ECM and facilitating the migration of immune cells to sites of inflammation. It also modulates the activity of inflammatory mediators, influencing the inflammatory response.
Clinical Implications
Given its role in cancer and inflammation, heparanase is a target for therapeutic intervention. Inhibitors of heparanase are being developed to prevent tumor metastasis and reduce inflammation. These inhibitors aim to block the enzymatic activity of heparanase, thereby preserving the integrity of the ECM and inhibiting the release of pro-tumorigenic and pro-inflammatory factors.
Research Directions
Current research is focused on understanding the regulation of heparanase expression and activity, as well as its interactions with other molecules in the ECM. Studies are also exploring the potential of heparanase inhibitors in clinical settings, particularly in cancer therapy.
Also see
| Enzymes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
| Overview of tumors, cancer and oncology (C00–D48, 140–239) | ||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Transform your life with W8MD's budget GLP-1 injections from $125.
W8MD offers a medical weight loss program to lose weight in Philadelphia. Our physician-supervised medical weight loss provides:
- Most insurances accepted or discounted self-pay rates. We will obtain insurance prior authorizations if needed.
- Generic GLP1 weight loss injections from $125 for the starting dose.
- Also offer prescription weight loss medications including Phentermine, Qsymia, Diethylpropion, Contrave etc.
NYC weight loss doctor appointments
Start your NYC weight loss journey today at our NYC medical weight loss and Philadelphia medical weight loss clinics.
- Call 718-946-5500 to lose weight in NYC or for medical weight loss in Philadelphia 215-676-2334.
- Tags:NYC medical weight loss, Philadelphia lose weight Zepbound NYC, Budget GLP1 weight loss injections, Wegovy Philadelphia, Wegovy NYC, Philadelphia medical weight loss, Brookly weight loss and Wegovy NYC
|
WikiMD's Wellness Encyclopedia |
| Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD